Associate Product Manager/Product Manager

Endovascular Engineering•Menlo Park, CA

2d•$100,000 - $150,000

About The Position

Endovascular Engineering (E2), a mission-driven venture-backed medical device company based in Menlo Park, California, develops clot-removal technologies for venous thromboembolism (VTE), pulmonary embolism (PE), and other vascular conditions. The Associate Product Manager/Product Manager supports product strategy and lifecycle management for the company’s mechanical thrombectomy platform, connecting clinical insight, engineering, and commercial execution. The role translates physician needs into product requirements and helps position the technology for treatment of patients with VTE. Leveling as Associate Product Manager or Product Manager depends on experience. The role works across product strategy and roadmap development, product development and lifecycle management, launch and commercial enablement, clinical and key opinion leader engagement, and cross-functional collaboration. It partners with R&D, clinical and medical teams, regulatory, quality, operations, and sales from early requirements through commercialization. The position is based in the United States and may require up to 30% travel for case coverage, conferences, physician engagement, and field partnership.

Requirements

1–5 years of experience.
Experience gathering user needs and translating them into product requirements within a design control environment.
Ability to work effectively with engineers and clinicians and translate between technical and clinical perspectives.
Strong understanding of physician decision-making, procedural workflow, and hospital purchasing dynamics.
Excellent project management, analytical, communication, and cross-functional collaboration skills.
Ability to operate independently with a high degree of ownership and accountability.
Familiarity with FDA design controls, regulatory requirements, and promotional compliance requirements for medical devices.
Bachelor’s degree required.
Based in the United States, with full work authorization and proximity to a major airport.

Nice To Haves

Medical device experience.
Vascular, interventional, or procedural experience.
Experience supporting product development and/or commercial launches in high-growth environments.
MBA or advanced degree.

Responsibilities

Develop and maintain a product roadmap aligned with clinical, commercial, and corporate priorities.
Collect market and user-needs input through physician interviews, case observation, field feedback, and competitive analysis.
Translate customer insights into product requirements, user needs, and design inputs in partnership with R&D.
Monitor competitors and market dynamics to inform product strategy, pricing, and investment decisions.
Represent the customer on cross-functional development teams from concept through launch.
Support design validation, usability studies, and clinical evaluations to confirm products meet physician and patient needs.
Manage product lifecycle activities, including line extensions, iterative improvements, and SKU and portfolio decisions.
Partner with Quality, Regulatory, and Operations on design controls, labeling, and post-market feedback.
Support or lead launch planning, including segmentation, positioning, messaging, and go-to-market readiness.
Develop product training, technical selling narratives, competitive positioning, and launch toolkits for field sales.
Support case coverage and field partnership to gather real-world feedback and drive adoption.
Collaborate with KOLs, advisors, and early adopters to capture procedural insights and validate product direction.
Support advisory boards, labs, and user feedback sessions.
Support the company’s presence at medical conferences, symposia, and product showcases.
Work with R&D, Clinical, Medical Affairs, Medical Education, Regulatory, Quality, and Sales to align work from requirements through commercialization.
Communicate product priorities, tradeoffs, and progress clearly to leadership and stakeholders.